An Analysis of Cellular Communication Network Factor Proteins as Candidate Mediators of Postpartum Psychosis Risk
Datos Bibliográficos
| ID | 15518853 |
|---|---|
| Autores | William Davies (0000-0003-1830-5403, Cardiff University, autor de correspondencia) |
| Año | 2019 |
| Volumen | 10 |
| Páginas | 876-876 |
| Fecha de publicación | 2019-11-26 |
| Peer Reviewed | Sí |
| Open Access | Sí |
| Tipo | ARTICLE |
| Revista | Frontiers in Psychiatry (JOURNAL) |
| Identificadores de la revista | ISSN: 1664-0640 • E-ISSN: 1664-0640 |
| Editorial | Frontiers Media (PUBLISHER • CH) |
| DOI | 10.3389/fpsyt.2019.00876 |
| PMID | 31849729 |
| OpenAlex | W2989787382 |
| Idioma | EN |
| Referencias citadas | 73 |
Postpartum (or puerperal) psychosis (PP) is a severe psychiatric condition associated with hallucinations, delusions, cognitive disorganization, and mood problems, which affects approximately 1-2 out of every 1,000 mothers shortly after childbirth. While the risk factors for, and co-morbidities of, PP are relatively well-defined, currently, the pathophysiology underlying the disorder is very poorly-specified. Here, I argue, on the basis of multiple lines of new evidence, that altered expression of the Cellular Communication Network (CCN) factor proteins (and of the heterodimerizing CCN2 and CCN3 proteins in particular), may be associated with, and possibly causal for, increased PP risk. Future preclinical and clinical studies should aim to test this hypothesis as empirical support for it would provide much-needed clues regarding the biological substrates of PP, and could point to predictive biomarkers for the condition
Anxiety · Bioinformatics · Biology · Mood · Mood disorders · Psychiatry · Psychosis · Risk factor · Schizophrenia (object-oriented programming · Clinical Psychology · Connective Tissue Growth Factor Research · Endometriosis Research and Treatment · Medicine · Neuroscience · Psychology · Wnt/β-catenin signaling in development and cancer · Internal Medicine
| Velocidad de citación | historical |
|---|---|
| Altamente citado | No |